FDA Inspection 1311716 — Gregory Manufacturing, Inc.

Gregory Manufacturing, Inc. — FEI 1000120897

The FDA completed an inspection of Gregory Manufacturing, Inc. on April 2, 2026 in Holyoke, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 2, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Holyoke, MA (United States)

Citations

IDCFRDescription
23255ISO 13485:2016 Clause 8.5.2Corrective action not taken